-
Je něco špatně v tomto záznamu ?
Suppression of peptide sample losses in autosampler vials
K. Stejskal, D. Potěšil, Z. Zdráhal,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
23590590
DOI
10.1021/pr400183v
Knihovny.cz E-zdroje
- MeSH
- adsorpce MeSH
- chromatografie kapalinová normy MeSH
- elektroforéza v polyakrylamidovém gelu MeSH
- formiáty MeSH
- hydrofobní a hydrofilní interakce MeSH
- močovina MeSH
- odběr biologického vzorku normy MeSH
- peptidové fragmenty izolace a purifikace normy MeSH
- polyethylenglykoly MeSH
- proteiny chemie MeSH
- průtoková injekční analýza normy MeSH
- thiomočovina MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Protein or peptide sample losses could accompany all steps of the proteomic analysis workflow. We focused on suppression of sample adsorptive losses during sample storage in autosampler vials. We examined suppression capabilities of six different sample injection solutions and seven types of autosampler vial surfaces using a model sample (tryptic digest of six proteins, 1 fmol per protein). While the vial material did not play an essential role, the choice of appropriate composition of sample injection solution reduced adsorptive losses substantially. The combination of a polypropylene vial and solution of poly(ethylene glycol) (PEG) (0.001%) or a mixture of high concentrated urea and thiourea (6 M and 1 M) as injection solutions (both acidified with formic acid (FA) (0.1%)) provided the best results in terms of number of significantly identified peptides (p < 0.05). These conclusions were confirmed by analyses of a real sample with intermediate complexity (in-gel digest from sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE)). Addition of PEG into the real sample solution proved to prevent higher losses, concerning mainly hydrophobic peptides, during up to 48 h storage in the autosampler in comparison with a formic acid solution and even with a solution of highly concentrated urea and thiourea. Using PEG for several months was not accompanied by any adverse effect to the liquid chromatography system.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc14040812
- 003
- CZ-PrNML
- 005
- 20140114113152.0
- 007
- ta
- 008
- 140107s2013 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1021/pr400183v $2 doi
- 035 __
- $a (PubMed)23590590
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Stejskal, Karel
- 245 10
- $a Suppression of peptide sample losses in autosampler vials / $c K. Stejskal, D. Potěšil, Z. Zdráhal,
- 520 9_
- $a Protein or peptide sample losses could accompany all steps of the proteomic analysis workflow. We focused on suppression of sample adsorptive losses during sample storage in autosampler vials. We examined suppression capabilities of six different sample injection solutions and seven types of autosampler vial surfaces using a model sample (tryptic digest of six proteins, 1 fmol per protein). While the vial material did not play an essential role, the choice of appropriate composition of sample injection solution reduced adsorptive losses substantially. The combination of a polypropylene vial and solution of poly(ethylene glycol) (PEG) (0.001%) or a mixture of high concentrated urea and thiourea (6 M and 1 M) as injection solutions (both acidified with formic acid (FA) (0.1%)) provided the best results in terms of number of significantly identified peptides (p < 0.05). These conclusions were confirmed by analyses of a real sample with intermediate complexity (in-gel digest from sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE)). Addition of PEG into the real sample solution proved to prevent higher losses, concerning mainly hydrophobic peptides, during up to 48 h storage in the autosampler in comparison with a formic acid solution and even with a solution of highly concentrated urea and thiourea. Using PEG for several months was not accompanied by any adverse effect to the liquid chromatography system.
- 650 _2
- $a adsorpce $7 D000327
- 650 _2
- $a chromatografie kapalinová $x normy $7 D002853
- 650 _2
- $a elektroforéza v polyakrylamidovém gelu $7 D004591
- 650 _2
- $a průtoková injekční analýza $x normy $7 D017022
- 650 _2
- $a formiáty $7 D005561
- 650 _2
- $a hydrofobní a hydrofilní interakce $7 D057927
- 650 _2
- $a peptidové fragmenty $x izolace a purifikace $x normy $7 D010446
- 650 _2
- $a polyethylenglykoly $7 D011092
- 650 _2
- $a proteiny $x chemie $7 D011506
- 650 _2
- $a odběr biologického vzorku $x normy $7 D013048
- 650 _2
- $a thiomočovina $7 D013890
- 650 _2
- $a močovina $7 D014508
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Potěšil, David $u -
- 700 1_
- $a Zdráhal, Zbyněk $u -
- 773 0_
- $w MED00166892 $t Journal of proteome research $x 1535-3907 $g Roč. 12, č. 6 (2013), s. 3057-62
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/23590590 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20140107 $b ABA008
- 991 __
- $a 20140114113856 $b ABA008
- 999 __
- $a ok $b bmc $g 1005208 $s 839324
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2013 $b 12 $c 6 $d 3057-62 $i 1535-3907 $m Journal of proteome research $n J Proteome Res $x MED00166892
- LZP __
- $a Pubmed-20140107